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2019-NCov Neutralizing Antibody Rapid Test Kit Double Check

    Buy cheap 2019-NCov Neutralizing Antibody Rapid Test Kit Double Check from wholesalers
     
    Buy cheap 2019-NCov Neutralizing Antibody Rapid Test Kit Double Check from wholesalers
    • Buy cheap 2019-NCov Neutralizing Antibody Rapid Test Kit Double Check from wholesalers

    2019-NCov Neutralizing Antibody Rapid Test Kit Double Check

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    Brand Name : Aichek
    Model Number : COVID-19-G02001A
    Certification : CE
    Price : 1.2 USD
    Payment Terms : T/T
    Supply Ability : negotiable
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    2019-NCov Neutralizing Antibody Rapid Test Kit Double Check

    2019-nCov neutralizing Antibody Rapid Test Kit double check for successful vaccination

    For professional and in vitro diagnostic use only.

    Product Name2019-nCov neutralizing Antibody Rapid Test Kit
    FormatsStrip(3mm)Device(4mm) uncut sheet
    Place of OrigenChina
    SpecimenBlood
    Read Time15 minutes
    Shelf life2 years
    Packageuncut sheet
    Storage2℃-30℃

    For professional and in vitro diagnostic use only.


    [INTENDED USE]


    The product is suitable for qualitative detection of neutralizing antibodies (NAbs) against SARS-CoV-2 that block the interaction between the receptor binding domain (RBD) of the spike glycoprotein and the Angiotensin converting enzyme Ⅱ (ACE2) receptor. The device can be instrumental in vaccine and therapeutic development as it is suitable for all antibody isotypes. It may also help in current COVID-19 investigations of sero-prevalence, assessment of human immunity, longevity of protective immunity, efficacy of different vaccine candidates as well as tracking infection.


    [PERFORMANCE CHARACTERISTICS]


    Sensitivity

    The sensitivity to S-mIgG1 neutralizing antibody can reach 2ug/mL.

    Accuracy

    A side-by-side comparison was conducted by the results of SARS-Cov-2 Neutralizing Antibody Test Device (Test Reagent) developed by Hangzhou Deangel Biological Engineering Co., Ltd. and cPassTM from Genscript CO., Ltd. 328 clinical specimens from Professional Point of Care site were evaluated, 105 were positive and others negative. Base on the results from the clinical studies, the statistical analysis was made as follows:

    cPassTMTotal
    PositiveNegative

    Test

    reagent

    Positive96298
    Negative9221230
    Total105223328

    For test reagent, the clinical sensitivity with the “Compared Reagent” was 91.4% (95% CI: 77.7%~100%), the clinical specificity was 99.1% (95% CI: 97.2%~100%), the coincidence rate was 96.6% (95% CI: 92.4%~100%).

    [SUMMARY]

    The novel coronaviruses belong to the β genus. COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel coronavirus are the main source of infection; asymptomatic infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main manifestations include fever, fatigue and dry cough. Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases.


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